NP-MRD: Showing NP-Card for (2r,3r,4s,5s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4s,5r,6s)-3,4,5-tris(acetyloxy)-6-{[(1r,2r)-2-(acetyloxy)-1-methyl-4-(propan-2-ylidene)cyclohexyl]oxy}oxan-2-yl]methoxy}oxan-3-yl acetate (NP0160198)

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Record Information

Version

2.0

Created at

2022-09-02 18:05:38 UTC

Updated at

2022-09-02 18:05:38 UTC

NP-MRD ID

NP0160198

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3r,4s,5s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4s,5r,6s)-3,4,5-tris(acetyloxy)-6-{[(1r,2r)-2-(acetyloxy)-1-methyl-4-(propan-2-ylidene)cyclohexyl]oxy}oxan-2-yl]methoxy}oxan-3-yl acetate

Description

(1R,2R)-2-methyl-5-(propan-2-ylidene)-2-{[(2S,3R,4S,5R,6R)-3,4,5-tris(acetyloxy)-6-({[(2R,3R,4S,5S)-3,4,5-tris(acetyloxy)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}cyclohexyl acetate belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. (2r,3r,4s,5s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4s,5r,6s)-3,4,5-tris(acetyloxy)-6-{[(1r,2r)-2-(acetyloxy)-1-methyl-4-(propan-2-ylidene)cyclohexyl]oxy}oxan-2-yl]methoxy}oxan-3-yl acetate is found in Physalis peruviana. Based on a literature review very few articles have been published on (1R,2R)-2-methyl-5-(propan-2-ylidene)-2-{[(2S,3R,4S,5R,6R)-3,4,5-tris(acetyloxy)-6-({[(2R,3R,4S,5S)-3,4,5-tris(acetyloxy)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}cyclohexyl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022220052D          

 53 55  0  0  1  0            999 V2000
   -2.4034    0.7223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4034   -0.1027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1178   -0.5152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6889   -0.5152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6889   -1.3402    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9744   -1.7527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9744   -2.5777    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6889   -2.9902    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6889   -3.8152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9744   -4.2277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2600   -3.8152    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2600   -2.9902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4545   -2.5777    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4545   -1.7527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1690   -1.3402    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4512   -2.1154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6387   -0.7082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9209    0.0670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7333    0.2103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0155    0.9855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4852    1.6175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8280    1.1288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2636   -0.4217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9815   -1.1969    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5118   -1.8289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3242   -1.6857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6064   -0.9104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8545   -2.3177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1690   -2.9902    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8835   -2.5777    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5979   -2.9902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5979   -3.8152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3124   -2.5777    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1690   -3.8152    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8835   -4.2277    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8835   -5.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5979   -5.4652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1690   -5.4652    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4545   -4.2277    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4545   -5.0527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2600   -5.4652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9744   -5.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2600   -6.2902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4034   -2.5777    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1178   -2.9902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1178   -3.8152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4034   -4.2277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8323   -4.2277    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4034   -1.7527    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1178   -1.3402    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8323   -1.7527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8323   -2.5777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5468   -1.3402    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
 11 10  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 15 14  1  6  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 19 23  1  0  0  0  0
 23 24  1  0  0  0  0
 15 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
 13 29  1  0  0  0  0
 29 30  1  6  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
 29 34  1  0  0  0  0
 34 35  1  1  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  2  0  0  0  0
 34 39  1  0  0  0  0
 11 39  1  0  0  0  0
 39 40  1  6  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  2  0  0  0  0
  8 44  1  0  0  0  0
 44 45  1  6  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  2  0  0  0  0
 44 49  1  0  0  0  0
  5 49  1  0  0  0  0
 49 50  1  1  0  0  0
 50 51  1  0  0  0  0
 51 52  1  0  0  0  0
 51 53  2  0  0  0  0
M  END

     RDKit          3D

103105  0  0  0  0  0  0  0  0999 V2000
   -5.4265    6.2657    1.7307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8565    5.2479    0.8199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5389    5.4920   -0.3637 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.1275    2.9241    0.5048 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7953    2.4456    1.0497 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3140    1.5534    0.0960 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9670    0.3626    0.2237 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2719   -0.4330    1.1229 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6859   -1.5474    0.6031 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6148   -1.3157   -0.4328 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3843   -0.5906    0.1382 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6588   -1.1119    0.0281 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4962   -0.4574    0.8608 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6395    0.1070    0.4159 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6155   -0.8427   -0.2321 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4136    0.5800    1.6794 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6556    1.2937    1.3153 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6034    2.1187    0.1139 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4486    3.1314   -0.0028 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4408    3.4319    1.0705 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4469    4.0030   -1.1975 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6447    1.8645   -0.9781 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3616    1.3507   -0.3481 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3288    1.2744   -1.3040 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2297    2.1552   -1.2589 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1381    2.0857   -2.2623 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1846    3.0140   -0.3444 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6041   -2.5708    0.5189 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9065   -3.0425    0.6515 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3718   -3.4199    1.8990 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7355   -3.9289    2.1273 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5869   -3.3197    2.8746 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.6239   -4.6177   -0.0771 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2475   -5.7396   -0.5646 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9047   -7.0602   -0.0180 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1016   -5.6502   -1.4659 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2418   -2.5958   -1.0891 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0878   -2.4408   -2.4999 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9042   -3.0505   -3.4358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7287   -2.8766   -4.8993 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8320   -3.7816   -2.9995 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4245    0.4398    0.5891 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.1150   -0.6034   -0.0757 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7253   -1.6617    0.5529 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4452   -2.7398   -0.2141 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6767   -1.7245    1.8089 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0740    1.7646    0.2969 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.1578    1.9474    1.1860 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4686    2.0547    0.8037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5913    2.2470    1.7645 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7539    1.9894   -0.4151 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.0971    3.3013    1.0976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9002    1.9391    2.0348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8970   -0.1382   -0.7883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3050   -2.1480    1.4685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4650   -2.2361    0.1469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0507   -0.6807   -1.2311 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9203   -1.1727   -1.0230 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2403   -1.3938   -1.0858 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4797   -0.2252   -0.5963 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0772   -1.4476    0.5799 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6248   -0.3046    2.3206 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7504    1.2492    2.2550 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4489    0.5073    1.1381 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0456    1.8898    2.1671 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2895    4.0381    0.6709 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8804    2.4954    1.4970 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0121    3.9910    1.9142 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7710    4.8754   -1.1009 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2154    3.3762   -2.0979 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4728    4.4267   -1.3468 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2089   -7.1822   -0.0423 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.1967   -1.9338   -5.1009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4876    0.2200    1.6750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5314   -2.6850   -0.0627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1508   -2.6250   -1.2971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0632   -3.7467    0.0717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4882    1.7301   -0.7298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2550    2.4439    2.7929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1649    1.2793    1.8032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3141    3.0145    1.4216 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
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  5  6  1  0
  6  7  1  0
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 13 14  1  0
 15 14  1  1
 15 16  1  0
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 19 23  1  0
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 25 26  1  0
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 19 20  2  3
 20 21  1  0
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 13 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 31 33  2  0
 29 34  1  0
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 35 36  1  0
 36 37  1  0
 36 38  2  0
 34 39  1  0
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  8 44  1  0
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 45 46  1  0
 46 47  1  0
 46 48  2  0
 44 49  1  0
 49 50  1  0
 50 51  1  0
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 51 53  2  0
 49  5  1  0
 39 11  1  0
 24 15  1  0
  1 54  1  0
  1 55  1  0
  1 56  1  0
  5 57  1  6
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  6 59  1  0
  8 60  1  6
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 10 62  1  0
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 16 67  1  0
 17 68  1  0
 17 69  1  0
 18 70  1  0
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 23 78  1  0
 23 79  1  0
 24 80  1  1
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 27 82  1  0
 27 83  1  0
 21 72  1  0
 21 73  1  0
 21 74  1  0
 22 75  1  0
 22 76  1  0
 22 77  1  0
 29 84  1  1
 32 85  1  0
 32 86  1  0
 32 87  1  0
 34 88  1  6
 37 89  1  0
 37 90  1  0
 37 91  1  0
 39 92  1  6
 42 93  1  0
 42 94  1  0
 42 95  1  0
 44 96  1  1
 47 97  1  0
 47 98  1  0
 47 99  1  0
 49100  1  6
 52101  1  0
 52102  1  0
 52103  1  0
M  END


  Mrv1652309022220052D          

 53 55  0  0  1  0            999 V2000
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   -2.4034   -0.1027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1178   -0.5152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6889   -0.5152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6889   -1.3402    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9744   -1.7527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9744   -2.5777    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6889   -2.9902    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6889   -3.8152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9744   -4.2277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2600   -3.8152    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2600   -2.9902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4545   -2.5777    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4545   -1.7527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1690   -1.3402    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4512   -2.1154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6387   -0.7082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.7333    0.2103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0155    0.9855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4852    1.6175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8280    1.1288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2636   -0.4217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9815   -1.1969    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5118   -1.8289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3242   -1.6857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6064   -0.9104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8545   -2.3177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1690   -2.9902    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8835   -2.5777    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5979   -2.9902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5979   -3.8152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3124   -2.5777    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1690   -3.8152    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8835   -4.2277    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8835   -5.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5979   -5.4652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1690   -5.4652    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4545   -4.2277    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4545   -5.0527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2600   -5.4652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9744   -5.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2600   -6.2902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4034   -2.5777    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1178   -2.9902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1178   -3.8152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4034   -4.2277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8323   -4.2277    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4034   -1.7527    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1178   -1.3402    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8323   -1.7527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8323   -2.5777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5468   -1.3402    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
 11 10  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 15 14  1  6  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 19 23  1  0  0  0  0
 23 24  1  0  0  0  0
 15 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
 13 29  1  0  0  0  0
 29 30  1  6  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
 29 34  1  0  0  0  0
 34 35  1  1  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  2  0  0  0  0
 34 39  1  0  0  0  0
 11 39  1  0  0  0  0
 39 40  1  6  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  2  0  0  0  0
  8 44  1  0  0  0  0
 44 45  1  6  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  2  0  0  0  0
 44 49  1  0  0  0  0
  5 49  1  0  0  0  0
 49 50  1  1  0  0  0
 50 51  1  0  0  0  0
 51 52  1  0  0  0  0
 51 53  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0160198

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@H]1CO[C@@H](OC[C@H]2O[C@@H](O[C@]3(C)CCC(C[C@H]3OC(C)=O)=C(C)C)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]2OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C35H50O18/c1-16(2)24-11-12-35(10,27(13-24)46-18(4)37)53-34-32(51-23(9)42)30(49-21(7)40)28(47-19(5)38)26(52-34)15-44-33-31(50-22(8)41)29(48-20(6)39)25(14-43-33)45-17(3)36/h25-34H,11-15H2,1-10H3/t25-,26+,27+,28+,29-,30-,31+,32+,33-,34-,35+/m0/s1

> <INCHI_KEY>
JJSFTGMVZVGDFG-YVYYGUCWSA-N

> <FORMULA>
C35H50O18

> <MOLECULAR_WEIGHT>
758.767

> <EXACT_MASS>
758.29971477

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
103

> <JCHEM_AVERAGE_POLARIZABILITY>
75.41054537839803

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3R,4S,5S)-4,5-bis(acetyloxy)-2-{[(2R,3R,4S,5R,6S)-3,4,5-tris(acetyloxy)-6-{[(1R,2R)-2-(acetyloxy)-1-methyl-4-(propan-2-ylidene)cyclohexyl]oxy}oxan-2-yl]methoxy}oxan-3-yl acetate

> <ALOGPS_LOGP>
2.34

> <JCHEM_LOGP>
1.2322775989999988

> <ALOGPS_LOGS>
-3.78

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.771461209508846

> <JCHEM_POLAR_SURFACE_AREA>
221.01999999999998

> <JCHEM_REFRACTIVITY>
172.48140000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
19

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.26e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R,4S,5S)-4,5-bis(acetyloxy)-2-{[(2R,3R,4S,5R,6S)-3,4,5-tris(acetyloxy)-6-{[(1R,2R)-2-(acetyloxy)-1-methyl-4-(propan-2-ylidene)cyclohexyl]oxy}oxan-2-yl]methoxy}oxan-3-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      -4.486   1.348   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.486  -0.192   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -5.820  -0.962   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -3.153  -0.962   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -3.153  -2.502   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.819  -3.272   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -1.819  -4.812   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -3.153  -5.582   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -3.153  -7.122   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -1.819  -7.892   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.485  -7.122   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -0.485  -5.582   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.848  -4.812   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       0.848  -3.272   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.182  -2.502   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.709  -3.949   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.192  -1.322   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.719   0.125   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.236   0.393   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.762   1.840   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.772   3.019   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.279   2.107   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.225  -0.787   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.699  -2.234   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.689  -3.414   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       6.205  -3.147   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.732  -1.699   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       7.195  -4.326   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       2.182  -5.582   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       3.516  -4.812   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       4.849  -5.582   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.849  -7.122   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       6.183  -4.812   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       2.182  -7.122   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       3.516  -7.892   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       3.516  -9.432   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       4.849 -10.202   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       2.182 -10.202   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       0.848  -7.892   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       0.848  -9.432   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      -0.485 -10.202   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -1.819  -9.432   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      -0.485 -11.742   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      -4.486  -4.812   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      -5.820  -5.582   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      -5.820  -7.122   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      -4.486  -7.892   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      -7.154  -7.892   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      -4.486  -3.272   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0      -5.820  -2.502   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0      -7.154  -3.272   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      -7.154  -4.812   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0      -8.487  -2.502   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   49                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   44                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   39                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   29                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17   24                                             
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   23                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   19   24                                                       
CONECT   24   23   15   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   13   30   34                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   29   35   39                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36                                                            
CONECT   39   34   11   40                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41                                                            
CONECT   44    8   45   49                                                  
CONECT   45   44   46                                                       
CONECT   46   45   47   48                                                  
CONECT   47   46                                                            
CONECT   48   46                                                            
CONECT   49   44    5   50                                                  
CONECT   50   49   51                                                       
CONECT   51   50   52   53                                                  
CONECT   52   51                                                            
CONECT   53   51                                                            
MASTER        0    0    0    0    0    0    0    0   53    0  110    0
END

View in JSmol

Synonyms

Value	Source
(1R,2R)-2-Methyl-5-(propan-2-ylidene)-2-{[(2S,3R,4S,5R,6R)-3,4,5-tris(acetyloxy)-6-({[(2R,3R,4S,5S)-3,4,5-tris(acetyloxy)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}cyclohexyl acetic acid	Generator

Chemical Formula

C₃₅H₅₀O₁₈

Average Mass

758.7670 Da

Monoisotopic Mass

758.29971 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@H]1CO[C@@H](OC[C@H]2O[C@@H](O[C@]3(C)CCC(C[C@H]3OC(C)=O)=C(C)C)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]2OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O

InChI Identifier

InChI=1S/C35H50O18/c1-16(2)24-11-12-35(10,27(13-24)46-18(4)37)53-34-32(51-23(9)42)30(49-21(7)40)28(47-19(5)38)26(52-34)15-44-33-31(50-22(8)41)29(48-20(6)39)25(14-43-33)45-17(3)36/h25-34H,11-15H2,1-10H3/t25-,26+,27+,28+,29-,30-,31+,32+,33-,34-,35+/m0/s1

InChI Key

JJSFTGMVZVGDFG-YVYYGUCWSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Physalis peruviana	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

O-glycosyl compounds

Alternative Parents

Substituents

O-glycosyl compound
Disaccharide
P-menthane monoterpenoid
Monoterpenoid
Monocyclic monoterpenoid
Oxane
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Acetal
Organic oxide
Hydrocarbon derivative
Carbonyl group
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	2.34	ALOGPS
logS	-3.8	ALOGPS

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163054176

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3r,4s,5s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4s,5r,6s)-3,4,5-tris(acetyloxy)-6-{[(1r,2r)-2-(acetyloxy)-1-methyl-4-(propan-2-ylidene)cyclohexyl]oxy}oxan-2-yl]methoxy}oxan-3-yl acetate (NP0160198)

MOL for NP0160198 ((2r,3r,4s,5s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4s,5r,6s)-3,4,5-tris(acetyloxy)-6-{[(1r,2r)-2-(acetyloxy)-1-methyl-4-(propan-2-ylidene)cyclohexyl]oxy}oxan-2-yl]methoxy}oxan-3-yl acetate)

3D MOL for NP0160198 ((2r,3r,4s,5s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4s,5r,6s)-3,4,5-tris(acetyloxy)-6-{[(1r,2r)-2-(acetyloxy)-1-methyl-4-(propan-2-ylidene)cyclohexyl]oxy}oxan-2-yl]methoxy}oxan-3-yl acetate)

3D SDF for NP0160198 ((2r,3r,4s,5s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4s,5r,6s)-3,4,5-tris(acetyloxy)-6-{[(1r,2r)-2-(acetyloxy)-1-methyl-4-(propan-2-ylidene)cyclohexyl]oxy}oxan-2-yl]methoxy}oxan-3-yl acetate)

3D-SDF for NP0160198 ((2r,3r,4s,5s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4s,5r,6s)-3,4,5-tris(acetyloxy)-6-{[(1r,2r)-2-(acetyloxy)-1-methyl-4-(propan-2-ylidene)cyclohexyl]oxy}oxan-2-yl]methoxy}oxan-3-yl acetate)

PDB for NP0160198 ((2r,3r,4s,5s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4s,5r,6s)-3,4,5-tris(acetyloxy)-6-{[(1r,2r)-2-(acetyloxy)-1-methyl-4-(propan-2-ylidene)cyclohexyl]oxy}oxan-2-yl]methoxy}oxan-3-yl acetate)

3D PDB for NP0160198 ((2r,3r,4s,5s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4s,5r,6s)-3,4,5-tris(acetyloxy)-6-{[(1r,2r)-2-(acetyloxy)-1-methyl-4-(propan-2-ylidene)cyclohexyl]oxy}oxan-2-yl]methoxy}oxan-3-yl acetate)

SMILES for NP0160198 ((2r,3r,4s,5s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4s,5r,6s)-3,4,5-tris(acetyloxy)-6-{[(1r,2r)-2-(acetyloxy)-1-methyl-4-(propan-2-ylidene)cyclohexyl]oxy}oxan-2-yl]methoxy}oxan-3-yl acetate)

INCHI for NP0160198 ((2r,3r,4s,5s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4s,5r,6s)-3,4,5-tris(acetyloxy)-6-{[(1r,2r)-2-(acetyloxy)-1-methyl-4-(propan-2-ylidene)cyclohexyl]oxy}oxan-2-yl]methoxy}oxan-3-yl acetate)

Structure for NP0160198 ((2r,3r,4s,5s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4s,5r,6s)-3,4,5-tris(acetyloxy)-6-{[(1r,2r)-2-(acetyloxy)-1-methyl-4-(propan-2-ylidene)cyclohexyl]oxy}oxan-2-yl]methoxy}oxan-3-yl acetate)

3D Structure for NP0160198 ((2r,3r,4s,5s)-4,5-bis(acetyloxy)-2-{[(2r,3r,4s,5r,6s)-3,4,5-tris(acetyloxy)-6-{[(1r,2r)-2-(acetyloxy)-1-methyl-4-(propan-2-ylidene)cyclohexyl]oxy}oxan-2-yl]methoxy}oxan-3-yl acetate)